Physicochemical, Pharmacokinetic, and Toxicity Evaluation of Methoxy Poly(ethylene glycol)- b -Poly(d,l-Lactide) Polymeric Micelles Encapsulating Alpinumisoflavone Extracted from Unripe Cudrania tricuspidata Fruit

Alpinumisoflavone, a major compound in unripe fruit is reported to exhibit numerous beneficial pharmacological activities, such as osteoprotective, antibacterial, estrogenic, anti-metastatic, atheroprotective, antioxidant, and anticancer effects. Despite its medicinal value, alpinumisoflavone is poo...

Full description

Saved in:
Bibliographic Details
Published in:Pharmaceutics 2019-08, Vol.11 (8), p.366
Main Authors: Jo, Min Jeong, Jo, Yang Hee, Lee, Yu Jin, Park, Chun-Woong, Kim, Jin-Seok, Hong, Jin Tae, Chung, Youn Bok, Lee, Mi Kyeong, Shin, Dae Hwan
Format: Article
Language:English
Subjects:
alpinumisoflavone
Cellulose
Cholesterol
Chromatography
Drugs
Estrogens
Fruits
Kinases
Metastasis
mPEG-b-PLA micelle
Particle size
Pharmaceuticals
Pharmacokinetics
Polymers
solubilization
Toxicity
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Alpinumisoflavone, a major compound in unripe fruit is reported to exhibit numerous beneficial pharmacological activities, such as osteoprotective, antibacterial, estrogenic, anti-metastatic, atheroprotective, antioxidant, and anticancer effects. Despite its medicinal value, alpinumisoflavone is poorly soluble in water, which makes it difficult to formulate and administer intravenously (i.v.). To overcome these limitations, we used methoxy poly(ethylene glycol)- -poly(d,l-lactide) (mPEG- -PLA) polymeric micelles to solubilize alpinumisoflavone and increase its bioavailability, and evaluated their toxicity in vivo. Alpinumisoflavone-loaded polymeric micelles were prepared using thin-film hydration method, and their physicochemical properties were characterized for drug release, particle size, drug-loading (DL, %), and encapsulation efficiency (EE, %). The in vitro drug release profile was determined and the release rate of alpinumisoflavone from mPEG- -PLA micelles was slower than that from drug solution, and sustained. Pharmacokinetic studies showed decreased total clearance and volume of distribution of alpinumisoflavone, whereas area under the curve (AUC) and bioavailability were significantly increased by incorporation in mPEG- -PLA micelles. In vivo toxicity assay revealed that alpinumisoflavone-loaded mPEG- -PLA micelles had no severe toxicity. In conclusion, we prepared an intravenous (i.v.) injectable alpinumisoflavone formulation, which was solubilized using mPEG- -PLA micelles, and determined their physicochemical properties, pharmacokinetics, and toxicity profiles.
ISSN:1999-4923
1999-4923
DOI:10.3390/pharmaceutics11080366